Mutagenesis Research Chemicals
Items 71 to 80 of 172 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Licochalcone A | 58749-22-7 | sc-319884 | 5 mg | $73.00 | 2 | |
Licochalcone A is a flavonoid compound that plays a notable role in mutagenesis research through its ability to modulate cellular pathways. It exhibits strong antioxidant properties, effectively scavenging free radicals and reducing oxidative damage to DNA. This compound influences gene expression by interacting with transcription factors, potentially altering cellular responses to stress. Its unique reactivity with biomolecules highlights its significance in studying mutagenic mechanisms and cellular integrity. | ||||||
Cordycepin | 73-03-0 | sc-203902 | 10 mg | $99.00 | 5 | |
Cordycepin is a nucleoside analog that serves as a pivotal tool in mutagenesis research due to its ability to interfere with RNA synthesis. By mimicking adenosine, it disrupts normal transcription processes, leading to altered gene expression and potential mutations. Its unique interaction with RNA polymerase can influence reaction kinetics, providing insights into the mechanisms of mutagenesis. Additionally, its structural properties allow for specific binding to nucleic acids, making it a valuable compound for studying genetic stability and cellular responses. | ||||||
Tetrabutylammonium Fluoride | 429-41-4 | sc-296487 sc-296487A | 25 ml 100 ml | $26.00 $58.00 | 1 | |
Tetrabutylammonium Fluoride is a versatile reagent in mutagenesis research, known for its ability to facilitate nucleophilic substitutions. Its unique quaternary ammonium structure enhances solubility in organic solvents, promoting efficient interactions with various substrates. The fluoride ion acts as a potent nucleophile, enabling the cleavage of carbon-fluorine bonds and influencing reaction pathways. This compound's distinct reactivity and ability to modulate ionic environments make it a significant tool for exploring genetic alterations and molecular dynamics. | ||||||
Cephalomannine | 71610-00-9 | sc-205626 sc-205626A sc-205626B sc-205626C | 5 mg 10 mg 1 g 2 g | $340.00 $490.00 $1400.00 $2000.00 | ||
Cephalomannine is a notable compound in mutagenesis research, characterized by its ability to interact with DNA and RNA through intercalation and groove binding. This interaction can induce structural changes in nucleic acids, potentially leading to mutagenic effects. Its unique stereochemistry allows for selective binding to specific sequences, influencing replication and transcription processes. Additionally, Cephalomannine's reactivity with cellular components can provide insights into mutagenesis mechanisms and genetic stability. | ||||||
Triflumuron | 64628-44-0 | sc-205873 sc-205873A | 10 g 25 g | $70.00 $122.00 | ||
Triflumuron is a distinctive chemical in mutagenesis research, known for its role as a chitin synthesis inhibitor. It disrupts the normal function of chitinase enzymes, leading to alterations in cellular integrity and growth patterns. This interference can trigger stress responses in organisms, potentially resulting in genetic mutations. Its unique interaction with chitin biosynthesis pathways offers valuable insights into the mechanisms of mutagenesis and the stability of genetic material. | ||||||
Tribromonitromethane | 464-10-8 | sc-396096 | 50 mg | $375.00 | ||
Tribromonitromethane is a notable compound in mutagenesis research, characterized by its ability to form reactive intermediates that can interact with nucleophilic sites in DNA. This interaction can lead to the formation of adducts, which may disrupt normal replication and transcription processes. Its distinct electrophilic nature allows it to participate in various reaction pathways, providing insights into mutagenic mechanisms and the stability of genetic information under stress conditions. | ||||||
(S)-6-Chloro-5-iodonicotine | 909193-59-5 | sc-396048 | 25 mg | $360.00 | ||
(S)-6-Chloro-5-iodonicotine is a significant compound in mutagenesis research, distinguished by its unique ability to engage in halogenation reactions that can modify nucleic acids. Its structural features facilitate specific interactions with DNA bases, potentially leading to strand breaks or cross-linking events. The compound's reactivity profile allows for the exploration of mutagenic pathways, shedding light on the mechanisms of genetic alteration and the resilience of cellular repair systems. | ||||||
S-(-)-Nicotine Di-p-Toluoyl-D-Tartrate Salt | 68935-26-2 | sc-394467 | 100 mg | $260.00 | ||
S-(-)-Nicotine Di-p-Toluoyl-D-Tartrate Salt serves as a pivotal tool in mutagenesis research, characterized by its capacity to form stable complexes with nucleophilic sites on biomolecules. This compound exhibits unique stereochemical properties that influence its interaction dynamics, potentially altering gene expression pathways. Its distinct reactivity can initiate oxidative stress responses, providing insights into mutagenic mechanisms and the cellular defense strategies against genetic damage. | ||||||
N,N′,N″,N‴,N⁗,N⁗′-Hexaacetylchitohexaose | 38854-46-5 | sc-222018 sc-222018A sc-222018B | 1 mg 5 mg 25 mg | $224.00 $408.00 $1846.00 | 3 | |
N,N',N'',N''',N'''',N'''''-Hexaacetylchitohexaose is a specialized compound in mutagenesis research, notable for its ability to interact with DNA and RNA through acetylation. This modification can influence the stability and conformation of nucleic acids, potentially affecting transcription and replication processes. Its unique structural features allow for selective binding to specific sites, facilitating the study of mutagenic pathways and the mechanisms of genetic alteration. | ||||||
Didox | 69839-83-4 | sc-221539 sc-221539A | 1 mg 5 mg | $20.00 $72.00 | ||
Didox is a distinctive compound utilized in mutagenesis research, characterized by its ability to intercalate within DNA structures. This intercalation can induce conformational changes, impacting the stability of the double helix and influencing replication fidelity. Its unique binding affinity allows for the exploration of mutagenic mechanisms, providing insights into genetic variability and the dynamics of nucleic acid interactions. The compound's reactivity with nucleophiles further enhances its role in studying mutagenesis pathways. | ||||||